TY - JOUR
T1 - Mechanistic perspectives on anti-aminoacyl-tRNA synthetase syndrome
AU - Kanaji, Sachiko
AU - Chen, Wenqian
AU - Morodomi, Yosuke
AU - Shapiro, Ryan
AU - Kanaji, Taisuke
AU - Yang, Xiang Lei
N1 - Funding Information:
We thank Dr Bernhard Kuhle for suggesting the existence of a C-end-rule peptide in the HisRS splice variant. We also thank the reviewers of this article for their insightful comments. The work is supported by National Institutes of Health grant R35 GM139627 to X.-L.Y. W.C. is supported by National Science Foundation fellowship 000894804 .
Publisher Copyright:
© 2022 Elsevier Ltd
PY - 2022
Y1 - 2022
N2 - Antisynthetase syndrome (ASSD) is an autoimmune disease characterized by circulating autoantibodies against one of eight aminoacyl-tRNA synthetases (aaRSs). Although these autoantibodies are believed to play critical roles in ASSD pathogenesis, the nature of their roles remains unclear. Here we describe ASSD pathogenesis and discuss ASSD-linked aaRSs – from the WHEP domain that may impart immunogenicity to the role of tRNA in eliciting the innate immune response and the secretion of aaRSs from cells. Through these explorations, we propose that ASSD pathogenesis involves the tissue-specific secretion of aaRSs and that extracellular tRNAs or tRNA fragments and their ability to engage Toll-like receptor signaling may be important disease factors.
AB - Antisynthetase syndrome (ASSD) is an autoimmune disease characterized by circulating autoantibodies against one of eight aminoacyl-tRNA synthetases (aaRSs). Although these autoantibodies are believed to play critical roles in ASSD pathogenesis, the nature of their roles remains unclear. Here we describe ASSD pathogenesis and discuss ASSD-linked aaRSs – from the WHEP domain that may impart immunogenicity to the role of tRNA in eliciting the innate immune response and the secretion of aaRSs from cells. Through these explorations, we propose that ASSD pathogenesis involves the tissue-specific secretion of aaRSs and that extracellular tRNAs or tRNA fragments and their ability to engage Toll-like receptor signaling may be important disease factors.
UR - http://www.scopus.com/inward/record.url?scp=85140342884&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85140342884&partnerID=8YFLogxK
U2 - 10.1016/j.tibs.2022.09.011
DO - 10.1016/j.tibs.2022.09.011
M3 - Review article
AN - SCOPUS:85140342884
SN - 0376-5067
JO - Trends in Biochemical Sciences
JF - Trends in Biochemical Sciences
ER -